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Year Number of Results
1999 1
2000 1
2001 2
2002 2
2003 1
2004 2
2007 1
2013 1
2014 1
2016 1
2017 3
2018 5
2019 4
2020 1
2021 5
2022 5
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40 results

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Page 1
Genetic epidemiology of inherited retinal diseases in a large patient cohort followed at a single center in Italy.
Karali M, Testa F, Di Iorio V, Torella A, Zeuli R, Scarpato M, Romano F, Onore ME, Pizzo M, Melillo P, Brunetti-Pierri R, Passerini I, Pelo E, Cremers FPM, Esposito G, Nigro V, Simonelli F, Banfi S. Karali M, et al. Among authors: pelo e. Sci Rep. 2022 Dec 2;12(1):20815. doi: 10.1038/s41598-022-24636-1. Sci Rep. 2022. PMID: 36460718 Free PMC article.
Large scale genome-wide association analyses identify novel genetic loci and mechanisms in hypertrophic cardiomyopathy.
Tadros R, Zheng SL, Grace C, Jordà P, Francis C, Jurgens SJ, Thomson KL, Harper AR, Ormondroyd E, West DM, Xu X, Theotokis PI, Buchan RJ, McGurk KA, Mazzarotto F, Boschi B, Pelo E, Lee M, Noseda M, Varnava A, Vermeer AM, Walsh R, Amin AS, van Slegtenhorst MA, Roslin N, Strug LJ, Salvi E, Lanzani C, de Marvao A; Hypergenes InterOmics Collaborators; Roberts JD, Tremblay-Gravel M, Giraldeau G, Cadrin-Tourigny J, L'Allier PL, Garceau P, Talajic M, Pinto YM, Rakowski H, Pantazis A, Baksi J, Halliday BP, Prasad SK, Barton PJ, O'Regan DP, Cook SA, de Boer RA, Christiaans I, Michels M, Kramer CM, Ho CY, Neubauer S; HCMR Investigators; Matthews PM, Wilde AA, Tardif JC, Olivotto I, Adler A, Goel A, Ware JS, Bezzina CR, Watkins H. Tadros R, et al. Among authors: pelo e. medRxiv [Preprint]. 2023 Feb 6:2023.01.28.23285147. doi: 10.1101/2023.01.28.23285147. medRxiv. 2023. PMID: 36778260 Free PMC article. Preprint.
Choroidal Caverns in Stargardt Disease.
Mucciolo DP, Giorgio D, Lippera M, Dattilo V, Passerini I, Pelo E, Sodi A, Virgili G, Giansanti F, Murro V. Mucciolo DP, et al. Among authors: pelo e. Invest Ophthalmol Vis Sci. 2022 Feb 1;63(2):25. doi: 10.1167/iovs.63.2.25. Invest Ophthalmol Vis Sci. 2022. PMID: 35156991 Free PMC article.
The Frequency of Intermediate Alleles in Patients with Cerebellar Phenotypes.
Capacci E, Bagnoli S, Giacomucci G, Rapillo CM, Govoni A, Bessi V, Polito C, Giotti I, Brogi A, Pelo E, Sorbi S, Nacmias B, Ferrari C. Capacci E, et al. Among authors: pelo e. Cerebellum. 2024 Jun;23(3):1135-1145. doi: 10.1007/s12311-023-01620-7. Epub 2023 Oct 31. Cerebellum. 2024. PMID: 37906407 Free PMC article.
Choroidal Vascularity Index in CHM Carriers.
Mucciolo DP, Giorgio D, Lippera M, Passerini I, Pelo E, Cipollini F, Sodi A, Virgili G, Giansanti F, Murro V. Mucciolo DP, et al. Among authors: pelo e. Front Ophthalmol (Lausanne). 2021 Oct 20;1:755058. doi: 10.3389/fopht.2021.755058. eCollection 2021. Front Ophthalmol (Lausanne). 2021. PMID: 38983966 Free PMC article.
En face OCT in choroideremia.
Murro V, Mucciolo DP, Sodi A, Giorgio D, Passerini I, Pelo E, Virgili G, Rizzo S. Murro V, et al. Among authors: pelo e. Ophthalmic Genet. 2019 Dec;40(6):514-520. doi: 10.1080/13816810.2019.1711429. Epub 2020 Jan 13. Ophthalmic Genet. 2019. PMID: 31928275
A genome-wide association study for survival from a multi-centre European study identified variants associated with COVID-19 risk of death.
Minnai F, Biscarini F, Esposito M, Dragani TA, Bujanda L, Rahmouni S, Alarcón-Riquelme ME, Bernardo D, Carnero-Montoro E, Buti M, Zeberg H, Asselta R, Romero-Gómez M; GEN-COVID Multicenter Study; Fernandez-Cadenas I, Fallerini C, Zguro K, Croci S, Baldassarri M, Bruttini M, Furini S, Renieri A, Colombo F. Minnai F, et al. Sci Rep. 2024 Feb 6;14(1):3000. doi: 10.1038/s41598-024-53310-x. Sci Rep. 2024. PMID: 38321133 Free PMC article.
Methimazole embryopathy: delineation of the phenotype.
Clementi M, Di Gianantonio E, Pelo E, Mammi I, Basile RT, Tenconi R. Clementi M, et al. Among authors: pelo e. Am J Med Genet. 1999 Mar 5;83(1):43-6. Am J Med Genet. 1999. PMID: 10076883 Review.
40 results